HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → isopropyl N-n-butoxymethyl-2-bromo-4-methyl-5-imidazolecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(Chloromethoxy)butane | HCID 11105357 | — |
| Reactant | HCID 178432453 | HCID 178432453 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | isopropyl N-n-butoxymethyl-2-bromo-4-methyl-5-imidazolecarboxylate | HCID 13589035 | 89% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a suspension of 293 milligrams (1.22 mM) of sodium hydride in 30 ml of anhydrous tetrahydrofuran was added, in portions, 3 g (1.22 mM) of isopropyl 2-bromo-4-methyl-5-imidazolecarboxylate. The resulting suspension was cooled to 0° C. and 1.5 g (1.22 mM) of chloromethyl-n-butyl ether was added dropwise. The reaction mixture was stirred overnight at room temperature. The precipitated sodium chloride was removed by filtration and concentration of the filtrate in vacuo gave 3.6 g of isopropyl N-n-butoxymethyl-2-bromo-4-methyl-5-imidazolecarboxylate as a golden oil (87%). Subsequent analysis indicated that the 3-isomer/1-isomer ratio was 91/9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04711962 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-89a68d88d12949dab80381831df1a89d |
| Source note | uspto-grants-1987_12 |